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2. Design multi-step syntheses for TWO of the following targets. Show the reagents needed for each...
4. (8 points) Devise multi-step syntheses for the following two targets. You must use the given starting materials as t...
4. (8 points) Devise multi-step syntheses for the following two targets. You must use the given starting materials as the only carbon source. You can use any other organic and inorganic reagents. steps a. V OH - starting material target
Design a multi-step synthesis for each of the following target molecules from the indicated starting material....
Design a multi-step synthesis for each of the following target molecules from the indicated starting material. Show the reagents needed for each step and the product of each step. Do not show any mechanisms. Draw the structures of the diene and the dienophile that reacted to form the Diels-Alder product shown. Provide the missing reagents in this multistep synthesis.
Propose multi-step chemical syntheses for the product on the right from the starting material provided, they...
Propose multi-step chemical syntheses for the product on the
right from the starting material provided, they require more than
one step. You can use any reagent with up to four carbons. Show the
product for each step in your synthesis.
5. 110 points] Chose TWO of the following transformations and propose multi-step chemical syntheses for the product on the right from the starting material provided. All syntheses require more than one step. You can use any reagent with up to...
Please explain the mechanisms! 1. Propose a synthesis for each of the following problems starting with reagent shown and using any other organic or inorganic reagents allowed in each problem. Mu...
Please explain the mechanisms!
1. Propose a synthesis for each of the following problems starting with reagent shown and using any other organic or inorganic reagents allowed in each problem. Multiple steps are required. The number of steps you use does not matter. Reactions should give the desired product as a major product. For full credit show the product of each step (reaction). If you make use of organometallic reagents such as Grignard, Wittig, organolithium, organosodium, organocopper, etc. you must...
5. 10 points Chose ONE of the following transformations and propose multi-step chemical syntheses for the...
5. 10 points Chose ONE of the following transformations and propose multi-step chemical syntheses for the product on the right from the starting material provided. All syntheses require more than one step. You can use any reagent with up to four carbons. Show the product for each step in your synthesis. Clearly indicate the problem that you do not wished graded with a giant X. HCCHE
Two Step Syntheses. You may use any inorganic reagent. You may use any organic reagent of...
Two Step Syntheses. You may use any inorganic reagent. You may use any organic reagent of two carbons or less. Assume major and minor products can be separated, but avoid minor products if possible. Option 1: Option 2: Option 3: OH Y OH 42
One-step synthesis: Design a synthesis, showing all of the reagents and products along the way. You...
One-step synthesis: Design a synthesis, showing all of the
reagents and products along the way. You may use any inorganic
reagent and any organic reagent of two carbons or less.
3) НО. НО ? + En
For 1 - 3, design reasonable syntheses of each of the target molecules using the provided...
For 1 - 3, design reasonable syntheses of each of the target molecules using the provided starting material and organic and inorganic reagents of your choice. Show the reagents needed for each step and the product of each step. Do not show any mechanisms. Please put all your answers on this sheet. Write your answers like this (actual number of starting steps may vary)material reagent(s) reagent(s) ABCD target Two equally reasonable routes are possible Can you find them both? (For...
Please answer question 4 with a full explanation. 4. (9 points) Multi-step synthesis. Devise a synthesis...
Please answer question 4 with a full explanation.
4. (9 points) Multi-step synthesis. Devise a synthesis for the target molecule starting from benzene and small alcohols with no more than two carbons. You can use any inorganic reagents necessary target 5. (10 points) Analysis of 'H NMR spectrum. Below is the 'H NMR spectrum of the product from this week's experiment.
2. Design concise syntheses for the following transformations. Show all reactants, reagents, products for each step...
2. Design concise syntheses for the following transformations. Show all reactants, reagents, products for each step a) and b) OH d) CN
4. (8 points) Devise multi-step syntheses for the following two targets. You must use the given starting materials as the only carbon source. You can use any other organic and inorganic reagents. steps a. V OH - starting material target
Design a multi-step synthesis for each of the following target molecules from the indicated starting material. Show the reagents needed for each step and the product of each step. Do not show any mechanisms. Draw the structures of the diene and the dienophile that reacted to form the Diels-Alder product shown. Provide the missing reagents in this multistep synthesis.
Propose multi-step chemical syntheses for the product on the
right from the starting material provided, they require more than
one step. You can use any reagent with up to four carbons. Show the
product for each step in your synthesis.
5. 110 points] Chose TWO of the following transformations and propose multi-step chemical syntheses for the product on the right from the starting material provided. All syntheses require more than one step. You can use any reagent with up to...
Please explain the mechanisms!
1. Propose a synthesis for each of the following problems starting with reagent shown and using any other organic or inorganic reagents allowed in each problem. Multiple steps are required. The number of steps you use does not matter. Reactions should give the desired product as a major product. For full credit show the product of each step (reaction). If you make use of organometallic reagents such as Grignard, Wittig, organolithium, organosodium, organocopper, etc. you must...
5. 10 points Chose ONE of the following transformations and propose multi-step chemical syntheses for the product on the right from the starting material provided. All syntheses require more than one step. You can use any reagent with up to four carbons. Show the product for each step in your synthesis. Clearly indicate the problem that you do not wished graded with a giant X. HCCHE
Two Step Syntheses. You may use any inorganic reagent. You may use any organic reagent of two carbons or less. Assume major and minor products can be separated, but avoid minor products if possible. Option 1: Option 2: Option 3: OH Y OH 42
One-step synthesis: Design a synthesis, showing all of the
reagents and products along the way. You may use any inorganic
reagent and any organic reagent of two carbons or less.
3) НО. НО ? + En
For 1 - 3, design reasonable syntheses of each of the target molecules using the provided starting material and organic and inorganic reagents of your choice. Show the reagents needed for each step and the product of each step. Do not show any mechanisms. Please put all your answers on this sheet. Write your answers like this (actual number of starting steps may vary)material reagent(s) reagent(s) ABCD target Two equally reasonable routes are possible Can you find them both? (For...
Please answer question 4 with a full explanation.
4. (9 points) Multi-step synthesis. Devise a synthesis for the target molecule starting from benzene and small alcohols with no more than two carbons. You can use any inorganic reagents necessary target 5. (10 points) Analysis of 'H NMR spectrum. Below is the 'H NMR spectrum of the product from this week's experiment.
2. Design concise syntheses for the following transformations. Show all reactants, reagents, products for each step a) and b) OH d) CN
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